Weinmann MEDUCORE Standard2 Instructions For Use Manual page 159

Alarm
Asystole
Defibrillation module defective
Device malfunction (display turns
yellow)
Check pad electrodes
(Manual mode)
Plug in pad connector
(Manual mode)
VF/VT*
11.2.2 Medium-priority alarm (yellow)
Alarm
Battery weak
NIBP diastolic
Cause
Asystole detected.
Internal defibrillation module
defective.
Temporary device malfunction.
Device defective.
Defibrillation electrodes not
attached or not correctly attached
to the patient.
Defibrillation electrodes not
connected or not correctly
connected to the trunk cable.
Trunk cable not connected or not
correctly connected to the device.
Ventricular fibrillation or
ventricular tachycardia detected.
* In the operator menu, the device can be preset so that the VF/VT
alarm can be deactivated and activated by the user. It can also be
preset in the operator menu whether the device is to start with an
activated or deactivated VF/VT alarm.
Cause
Low battery status.
Measured diastolic blood pressure
is above the set upper alarm limit.
11 Alarms and faults
Remedy
Proceed according to the latest
resuscitation guidelines.
If medically indicated, perform
suitable treatment.
Have the device repaired.
• Switch device off and back on
again.
• Perform a function check.
Have the device repaired.
Attach defibrillation electrodes to
the patient correctly
57).
Connect the pad connector on the
trunk cable correctly to the device
(see 4.4, p.
Connect the trunk cable correctly
to the device
Proceed according to the latest
resuscitation guidelines.
Switch to the AED mode or the
manual mode and perform
defibrillation, if medically
indicated (see 5.5, p.
Remedy
Replace battery
or connect device to the line power
(see 4.2, p.
If medically indicated, perform
suitable treatment or adapt the
alarm limits
MEDUCORE Standard
(see 4.4, p.
57).
(see 4.4, p. 57).
80).
(see 4.3.4, p. 56)
53).
(see 7.3.1, p. 111).
2
EN 159